E2E Supply Planner

Johnson & Johnson

E2E Supply Planner at Johnson & Johnson, overseeing clinical supplies for innovative medicine. Responsible for supply planning and ensuring compliance with regulatory standards.

Posted 7/7/2026full-timeBeerse • 🇧🇪 BelgiumMid-LevelSenior💰 €60,000 - €96,255 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in clinical supply planning and management, ensuring compliance with GMP guidelines while optimizing supply strategies for clinical trials. Strong leadership and communication skills are essential for driving process improvements and managing cross-functional projects.

Highest-signal resume keywords

Clinical Supply PlanningGMP ComplianceSupply Chain ManagementLeadership SkillsInventory Management

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Supply PlanningProduction PlanningLean6SigmaRoot Cause AnalysisData AnalysisClinical Demand AggregationProcess ImprovementDatabase MaintenanceProtocol Evaluation

Soft Skills

Excellent CommunicationNegotiation SkillsInfluencing SkillsMulti-taskingInnovative Thinking

Tools & Technologies

OMPSAP R/3ERP Systems

Industry Keywords

Clinical TrialsPharmaceutical IndustryQuality Management SystemsQ&C Requirements

Tech Stack

Tools & technologies

ERP

About the role

Key responsibilities & impact

Plans and manages the day-to-day activities of Clinical Supplies department such as packaging, labeling, assembling and shipping of clinical supplies used in clinical trials.
Responsible for the department's clinical supplies database records maintenance, protocol evaluation, coding of samples, and storage of approved materials.
Complies to local regulatory and good manufacturing practices guidelines.
Develop E2E supply plans for clinical compounds.
Identify the underlying assumptions for Kit/DP/API supply plan through the cS&OP process.
Develop optimal end-to-end drug product and drug substance supply strategies for compounds that minimize waste while meeting the timelines and needs of the Clinical Trial Material supply plans.
Create drug product and drug substance supply plans by aggregating clinical demand across different trials as well as non-clinical demands, to ensure timely delivery, testing and release of clinical batches.
Provide information to the Supply Network Capacity Planners and Plant Schedulers to allow constrained master and/or detailed scheduling of batches in the CSC supply network in line with the trial requirements and in line with critical raw material and component availability.
Drive structured improvements of functional processes in line with business or operational strategy.
Ensure portfolio timelines and business performance goals, objectives and metrics are achieved, including consistency with GMP guidelines and all other compliance requirements.
Lead and/or supporting cross-functional and cross-departmental projects to improve business process/tools.

Requirements

What you’ll need

A minimum of 3 years of related experience is required.
A minimum of a Bachelor’s Degree in business or science is required.
Experience with several of the following supply planning processes: inventory management, supply chain management, supply planning, production planning, Lean and 6sigma, systems (OMP, SAP R/3 or ERP), other cross-functional supply chain processes is required.
Strong leadership skills: Managing complexity, conflict, and ability to identify process gaps based on data or root cause analysis, ability to predict risk/impact of supply related processes are required.
Excellent communication, negotiation and influencing skills, with the ability to communicate clearly and appropriately to all levels of the organization in both written & oral forms is required.
The ability to work independently, multi-task and manage complexity is required.
An innate aim to make the difference and achieve results is required.
Continuous improvement in attitude and innovative thinking that will help see opportunities and related business needs is required.
Insight into a clinical supply environment in a pharmaceutical industry, its characteristics and constraints and Q&C requirements is preferred.
Experience with GMP and/or Quality management systems and processes is preferred.

Benefits

Comp & perks

an annual bonus with set target (% of pay) depending on pay grade / location, where the actual amount is based on the employees’ and companies’ performance of the previous calendar year, or sales commissions.
vacation days
parental leave for a minimum of 12 weeks
bereavement leave
caregiver leave
volunteer leave
well-being reimbursement
programs for financial, physical and mental health
service anniversary and recognition awards
eligibility for several insurance plans